CH239343A - Process for the preparation of a new polyazo dye. - Google Patents
Process for the preparation of a new polyazo dye.Info
- Publication number
- CH239343A CH239343A CH239343DA CH239343A CH 239343 A CH239343 A CH 239343A CH 239343D A CH239343D A CH 239343DA CH 239343 A CH239343 A CH 239343A
- Authority
- CH
- Switzerland
- Prior art keywords
- hol
- amino
- new
- carboxylic acid
- dye
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
- C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
- C09B43/16—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents linking amino-azo or cyanuric acid residues
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 237397. Verfahren zur Herstellung eines neuen Polyazofarbstoffes. Es wurde gefunden, dass man einen neuen Polyazofarbstoff erhält, wenn man 1 Hol di- a.zotierte 1-Amino-4,6-dichlorbenzol-2-carbon- säure, 1 Hol 2-Amino-5-oxynaphthalin-7-sul- fonsäure, 1 Hol Cyanurchlorid und 2 Hol 4- Amino -4'-oxy - 1,
1'- azobenzol - 3'- carbonsäure derart aufeinander einwirken lässt, dass die Diazoverbindung in & Stellung des Naphtha linkerns eingreift, und das Cyanurchlorid die A.minogruppe des Naphthalinderivates und diejenigen der beiden Aminoazofarbstoffe unter Bildung eines ternären Triazinkonden- sationsproduktes vereinigt.
Der neue Farbstoff stellt ein dunkel- btuunes Pulver dar und färbt Baumwolle in sehwach alkalischem Bade, das mit einer Kupfersalzlösung aus Kupfersulfat und wein saurem Natrium versetzt wurde, in wasch und lichtechten orangebraunen Tönen an.
<I>Beispiel:</I> 20,6 Gewichtsteile 1-Amino-4,6-dichlor- benzol-2-carbonsäure werden in 200 Gewichts teilen Wasser auf 40 erwärmt, 27 Gewichts- teile konzentrierte Salzsäure zugegeben, mit Eis auf 5 gekühlt und mit 6,9 Gewichtsteilen Natriumnitrit diazotiert. Die klare Diazo- lösung wird mit $2,1 Gewichtsteilen des in bekannter Weise hergestellten Triazinpro- duktes aus 1 Hol Cyanurchlorid, 1 Hol 2- Amino- 5 - oxynaphthalin-7-sulfonsäure,
und 2 Hol 4-Amino-4'-oxy-1,1'-azobenzol-3'-car- bonsäure, das in 1200 Teilen Wasser unter Zusatz von 60 Gewichtsteilen Natriumcarbo- riat gelöst wurde, gekuppelt. Man rührt einige Stunden und fällt den gebildeten Farbstoff mit Kochsalz.
Additional patent to main patent No. 237397. Process for the production of a new polyazo dye. It has been found that a new polyazo dye is obtained if 1 hol of di- a.zotierte 1-amino-4,6-dichlorobenzene-2-carboxylic acid, 1 hol of 2-amino-5-oxynaphthalene-7-sul- fonsäure, 1 hol cyanuric chloride and 2 hol 4- Amino -4'-oxy - 1,
1'-azobenzene-3'-carboxylic acid can act on each other in such a way that the diazo compound intervenes in the & position of the naphtha linker, and the cyanuric chloride combines the amino group of the naphthalene derivative and those of the two aminoazo dyes to form a ternary triazine condensation product.
The new dye is a dark blue powder and dyes cotton in a weakly alkaline bath to which a copper salt solution of copper sulfate and acidic sodium has been added in washable, lightfast orange-brown tones.
<I> Example: </I> 20.6 parts by weight of 1-amino-4,6-dichlorobenzene-2-carboxylic acid are heated to 40 in 200 parts by weight of water, 27 parts by weight of concentrated hydrochloric acid are added, with ice to 5 cooled and diazotized with 6.9 parts by weight of sodium nitrite. The clear diazo solution is mixed with $ 2.1 parts by weight of the triazine product prepared in a known manner from 1 part of cyanuric chloride, 1 part of 2-amino-5-oxynaphthalene-7-sulfonic acid,
and 2 hol 4-amino-4'-oxy-1,1'-azobenzene-3'-carboxylic acid, which was dissolved in 1200 parts of water with the addition of 60 parts by weight of sodium carbonate, coupled. The mixture is stirred for a few hours and the dyestuff formed is precipitated with sodium chloride.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH239343T | 1943-06-25 | ||
CH237397T | 1943-06-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH239343A true CH239343A (en) | 1945-09-30 |
Family
ID=25728254
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH239343D CH239343A (en) | 1943-06-25 | 1943-06-25 | Process for the preparation of a new polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH239343A (en) |
-
1943
- 1943-06-25 CH CH239343D patent/CH239343A/en unknown
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